Silodosin, Tadalafil Alone vs. Silodosin Plus Tadalafil as MET for Lower Ureteric Stones

Sponsor
Benha University (Other)
Overall Status
Completed
CT.gov ID
NCT05789732
Collaborator
(none)
168
1
4
5
33.4

Study Details

Study Description

Brief Summary

This study will compare the efficacy of silodosin, tadalafil versus silodosin plus tadalafil as Medical Expulsive Therapy (MET) for lower ureteric stones.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

The global incidence of urolithiasis, a disease with a high recurrence rate, is increasing. Urolithiasis is one of the most common disorders of the urinary tract with a lifetime prevalence of up to 15% with men affected three times more than women.

Urolithiasis causes recurrent stone formers to experience a decline in quality of life, and there is an increasing socioeconomic burden associated with the management of urolithiasis. Improved quality of life may also have increased its prevalence. A significant proportion, about 1/5th of urinary tract stones, is found in the ureter, of which 2/3rd is seen in the distal ureter. Initially, a colicky pain of various grades presents with ureteric stone. It is one of the most common problems that compel a patient to an emergency room.

Methods to manage ureteral stones include conservative treatment, pharmacological treatment (e.g., medical expulsive therapy), shock wave lithotripsy, and surgical treatment. Thus, urologists must select the appropriate treatment for each patient (i.e., non-surgical or surgical). Today, medical expulsive therapy has become the most used modality of treatment for urolithiasis. During this treatment, the ureter smooth muscle is treated via various drugs by different mechanisms.

Blocking alpha-(α-) 1 adrenergic receptor, especially in the distal third decreases basal smooth muscle contraction and causes propulsive antegrade peristalsis helping stone expulsion. By increasing the intraureteral pressure gradient around the stone, alpha-1 adrenergic receptor antagonists eject distal ureteral stones.

Significant pathological changes can occur when ureteric stones are impacted. +is can cause an inflammatory reaction with mucosal edema which could further worsen the ureteric obstruction, increasing the risk of impaction and retention. However, selective alpha-1 blockers, such as tamsulosin and silodosin, have been the treatment of choice, with proven efficacy in multiple clinical trials. Silodosin is a more selective α-1A adrenoceptor blocker with a better stone expulsion rate than tamsulosin.

Recently, a newer Phosphodiesterase type 5 inhibitor, tadalafil, has shown action on the nitric oxide-cyclic guanosine monophosphate signaling pathway of smooth muscles, resulting in increased levels of cyclic guanosine monophosphate, causing ureteric relaxation.

Due to its smooth muscle relaxation mechanism, tadalafil has received US Food and Drug Administration approval to treat many urinary tract diseases. Therefore, the combination of silodosin and tadalafil drugs is aimed to facilitate stone passage by better ureteric relaxation and reducing intramural ureter pressure. Although there have been few similar studies using various combinations, comparing the efficacy of silodosin and tadalafil vs. silodosin are very few, and these studies have taken longer duration of treatment (4 to 6 weeks) which might have affected the outcome.

Study Design

Study Type:
Interventional
Actual Enrollment :
168 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Treatment
Official Title:
Efficacy of Silodosin, Tadalafil Alone Versus Silodosin Plus Tadalafil as Medical Expulsive Therapy for Lower Ureteric Stones: A Prospective Randomized Placebo Controlled Study
Actual Study Start Date :
Mar 30, 2022
Actual Primary Completion Date :
Aug 30, 2022
Actual Study Completion Date :
Aug 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Placebo group

Patients in this group will receive placebo treatment once daily.

Drug: Placebo
Patients will receive placebo treatment once daily.

Experimental: Silodosin group

Patients will receive Silodosin 8 mg once daily.

Drug: Silodosin
Patients will receive Silodosin 8 mg once daily.

Experimental: Tadalafil group

Patients will receive Tadalafil 5 mg once daily.

Drug: Tadalafil
Patients will receive Tadalafil 5 mg once daily.

Experimental: Silodosin and Tadalafil

Patients will receive Silodosin 8mg in combination with Tadalafil 5 mg once daily.

Drug: Silodosin and Tadalafil
Patients will receive Silodosin 8mg in combination with Tadalafil 5 mg once daily.

Outcome Measures

Primary Outcome Measures

  1. Stone expulsion rate [Intraoperatively]

    Stone expulsion rate will be recorded

Secondary Outcome Measures

  1. Stone expulsion time [Intraoperatively]

    Stone expulsion time will be recorded

  2. Amount of analgesia used [Intraoperatively]

    The amount of analgesia used will be recorded

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 168 patients aged >18 years old.

  • Both sexes.

  • Diagnosed with lower ureteric stone from 5mm to 10mm in size.

Exclusion Criteria:
  • Patients with multiple or bilateral ureteric stones

  • single kidney or impairment of renal function

  • Urinary tract infection (UTI)

  • Marked hydronephrosis

  • Patients presenting with severe intractable pain and requiring emergency intervention

  • Any urologic anomalies or history of ureteral surgery

  • Pregnancy

  • Pediatric populations

  • Ischemic heart disease

  • Congestive cardiac failure

  • Complicated hypertension

  • Patients on concomitant treatment with nitrates or calcium channel blockers.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Benha University Hospitals Benha Egypt

Sponsors and Collaborators

  • Benha University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tamer Abd El-Wahab Diab, Lecturer of Urology, Faculty of Medicine, Benha University, Benha, Egypt, Benha University
ClinicalTrials.gov Identifier:
NCT05789732
Other Study ID Numbers:
  • Rc 22-3-2023
First Posted:
Mar 29, 2023
Last Update Posted:
Mar 31, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 31, 2023